P Moons
Katholieke Universiteit Leuven
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Publication
Featured researches published by P Moons.
Heart | 2005
P Moons; K Van Deyk; S. De Geest; Marc Gewillig; Werner Budts
Objective: To explore whether the severity of congenital heart disease is associated with the quality of life and perceived health status of adult patients. Design: Descriptive, cross sectional study. Setting: Adult congenital heart disease programme in one tertiary care centre in Belgium. Patients: 629 patients (378 men, 251 women) with a median age of 24 years. Main outcome measures: Disease severity was operationalised in terms of initial diagnosis (classification of Task Force 1 of the 32nd Bethesda Conference), illness course (disease severity index), and current functional status (New York Heart Association (NYHA) class, ability index, congenital heart disease functional index, and left ventricular ejection fraction). Quality of life was measured by a linear analogue scale, the satisfaction with life scale, and the schedule for evaluation of individual quality of life. Perceived health status was also assessed with a linear analogue scale. Results: Scores derived from the disease severity classification systems were weakly negatively associated with quality of life and health status, ranging from −0.05 to −0.27. The NYHA functional class and ability index were consistently associated with quality of life and perceived health. Conclusions: This study showed that the severity of congenital heart disease is marginally associated with patients’ quality of life and perceived health. Functional status was more related to patients’ assessment of their quality of life than was the initial diagnosis or illness course.
Archive | 1999
P Moons; S. Fairchild; S. De Geest
Quality of life has emerged as an important outcome measure in health care over the past two decades, and is increasingly used to evaluate treatment options. Indeed, understanding the quality of life implications of a new treatment modality in addition to studying its effects in terms of incidence of complications and mortality rate provides a more sophisticated and balanced view of treatment effects. Quality of life data offer a more complete understanding of the benefit/burden ratio associated with medical treatments in terms of patients’ physical, emotional/mental and social functioning.
European Journal of Cardiovascular Nursing | 2008
Åsa Axelsson; Bengt Fridlund; P Moons; J Mårtensson; Trijntje Jaarsma; K Smith; Anna Strömberg; David R. Thompson; Tone M. Norekvål
the problem-solving process are central. An integration of different areas of knowledge, theoretical as well as clinical can be used. Motivation can be seen as an important factor for adherence. Drieschner et al (2004) have described 6 internal determinants for treatment motivation; problem recognition, level of suffering, external pressure, perceived cost of treatment, perceived suitability of treatment, and outcome expectancy. These determinants as well as Selfdetermination theory (Decci & Ryan 2000) have been used as the base to develop an educational program using PBL to create motivation to engage in CPAP treatment.
Clinical Transplantation | 2008
Gerda Drent; P Moons; S. De Geest; Jan H. Kleibeuker; Eb Haagsma
Abstract: Symptom experience (occurrence and perceived distress) associated with side effects of immunosuppressive medications in organ transplant patients may well be associated with poorer quality of life and medication non‐compliance. The aims of this study were: first, to assess symptom experience in clinically stable adult patients during long‐term follow‐up after liver transplantation; and second, to study the relationship between symptom experience and medication non‐compliance. This cross‐sectional study included 123 liver transplant patients. Symptom experience was assessed using the “Modified Transplant Symptom Occurrence and Symptom Distress Scale” (29‐item version) at the annual evaluation. According to the duration of follow‐up, patients were divided into a short‐term (1–4 yr) and a long‐term (5–18 yr) cohort. Medication non‐compliance was measured using electronic monitoring. Results showed that increased hair growth was the most frequent symptom in both sexes. Symptom distress was more serious in women than in men. The most distressing symptom in women was excessive and/or painful periods, while in men this was impotence. Clear differences were revealed at item level between symptom occurrence and symptom distress in relationship with the two time cohorts and between sexes. No relationship was found between symptom experience and prednisolone non‐compliance.
Clinical Transplantation | 2008
Gerda Drent; P Moons; S. De Geest; Jan H. Kleibeuker; Eb Haagsma
Abstract: Symptom experience (occurrence and perceived distress) associated with side effects of immunosuppressive medications in organ transplant patients may well be associated with poorer quality of life and medication non‐compliance. The aims of this study were: first, to assess symptom experience in clinically stable adult patients during long‐term follow‐up after liver transplantation; and second, to study the relationship between symptom experience and medication non‐compliance. This cross‐sectional study included 123 liver transplant patients. Symptom experience was assessed using the “Modified Transplant Symptom Occurrence and Symptom Distress Scale” (29‐item version) at the annual evaluation. According to the duration of follow‐up, patients were divided into a short‐term (1–4 yr) and a long‐term (5–18 yr) cohort. Medication non‐compliance was measured using electronic monitoring. Results showed that increased hair growth was the most frequent symptom in both sexes. Symptom distress was more serious in women than in men. The most distressing symptom in women was excessive and/or painful periods, while in men this was impotence. Clear differences were revealed at item level between symptom occurrence and symptom distress in relationship with the two time cohorts and between sexes. No relationship was found between symptom experience and prednisolone non‐compliance.
Archive | 2008
Anja Declercq; Christiane Gosset; B Paepen; Johanna De Almeida Mello; Dirk Vanneste; Elke Detroyer; Koen Milisen; P Moons; J Berden; Joëlle Collard; Aurélie Londot; I Schumacher; N Demul; N Piette; T Joiris; Nicolas Gillain; C Van Audenhove
Archive | 2011
Anja Declercq; Johan Flamaing; Christiane Gosset; Koen Milisen; P Moons; Joëlle Collard; Samuel Delye; Els Devriendt; Nicolas Gillain; Aurélie Londot; L Van Eenoo; Dirk Vanneste; L Vesentini; Nathalie Wellens
Archive | 2010
Anja Declercq; Christiane Gosset; Johanna De Almeida Mello; Elke Detroyer; Nele Spruytte; Dirk Vanneste; L Vesentini; L Grevendonck; S Roovers; B Paepen; J Berden; Joëlle Collard; N Grauwels; Aurélie Londot; Claire Lepère; J Michel; Florence Renard; I Schumacher; Annalisa Tancredi; Nicolas Gillain; Nathalie Wellens; Koen Milisen; P Moons; C Van Audenhove
American Journal of Transplantation | 2005
S. De Geest; A Desmyttere; Kris Denhaerynck; Fabienne Dobbels; P Moons; James B. Young; Bonita Siegal; S Greenstein; Jürg Steiger; Yves Vanrenterghem; Jean-Paul Squifflet; J.P. van Hooff
Acta Hospitalia | 2005
P Moons; R. Cnutz; W. Decat; Goeminned; N. Halans; J. Verbeke; R. Verdoodt; K. Marquet; Nathalie Pasquasy; Christiane Gosset